Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs77409459
rs77409459
CFTR
4 0.851 0.160 7 117540243 missense variant C/T snv 2.8E-05 1.4E-05 0.800 1.000 37 1990 2015